4282-78-4 (孟鲁司特钠顺式异构体,N-Propargyl Phenothiazine)

CAS号:
4282-78-4
中文名称:
孟鲁司特钠顺式异构体
英文名称:
N-Propargyl Phenothiazine
分子式:
C15H11NS
分子量:
237.319542169571

孟鲁司特钠顺式异构体(4282-78-4)名称与标识符

名称

中文别名:
N-炔丙基吩噻嗪;孟鲁司特钠顺式异构体;异丙嗪杂质6;
英文别名:
N-Propargyl Phenothiazine;10-(2-Propyn-1-yl)-10H-phenothiazine;10-PROPARGYLPHENOTHIAZINE;N-Propargyl Phenothi;10-prop-2-ynylphenothiazine;Promethazine Impurity 6;10-(2-Propyn-1-yl)-10H-phenothiazine (ACI);10H-Phenothiazine, 10-(2-propynyl)- (9CI);Phenothiazine, 10-(2-propynyl)- (6CI, 7CI, 8CI);N-Propargylphenothiazine;

标识符

InChIKey:
HKJXSXLOBLUWBF-UHFFFAOYSA-N
Inchi:
1S/C15H11NS/c1-2-11-16-12-7-3-5-9-14(12)17-15-10-6-4-8-13(15)16/h1,3-10H,11H2
SMILES:
C#CCN1C2C(=CC=CC=2)SC2C1=CC=CC=2

孟鲁司特钠顺式异构体(4282-78-4)物化性质

实验特性

  • LogP : 3.98750
  • PSA : 28.54000

计算特性

  • 精确分子量 : 237.06100

孟鲁司特钠顺式异构体(4282-78-4)推荐厂家 更多厂家(3)

公司名称手机号/电话联系人QQ微信询单
上海楷森生物科技有限公司 17558870519
175-58870519
赵经理 3003926540
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深圳振强生物技术有限公司 13670046396
86-755-66853366
颜经理 2851296953
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湖北扬信医药科技有限公司 18672007304李玉婷 3003337926
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孟鲁司特钠顺式异构体(4282-78-4)合成路线

合成路线:1 步
反应条件:
参考文献:
Accessing Heteroannular Benzoxazole and Benzimidazole Scaffolds via Carbodiimides Using Azide-Isocyanide Cross Coupling as Catalyzed by Mesoionic Singlet Palladium Carbene Complexes Derived from Phenothiazine Moiety
Dey, Shreyata ; Ghosh, Prasenjit, ACS Omega, 2023, 8(12), 11039-11064
合成路线:1 步
反应条件:
参考文献:
Renewable SiO2 as support for NiO catalyst for regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles from azide-alkyne cycloaddition in aqueous media
Boggala, Sasikumar; Perupogu, Vijayanand; Varimalla, Shirisha; Manda, Kalpana; Akula, Venugopal, Molecular Catalysis, 2022, 521,
合成路线:1 步
反应条件:
参考文献:
Sugar-urea-salt eutectic mixture as an efficient green solvent for N-alkylation of heterocyclic secondary amines
Kumar, Koravangala S. Vinay; Swaroop, Toreshettahally R.; Ravi Singh, Krishna; Rangappa, Kanchugarakoppal S.; Sadashiva, Maralinganadoddi P., Chemical Data Collections, 2020, 29,
合成路线:1 步
反应条件:
参考文献:
One-Pot Regioselective Synthesis of Some Novel Isoxazole-Phenothiazine Hybrids and Their Antibacterial Activity
Guguloth, V.; Paidakula, S.; Vadde, R., Russian Journal of General Chemistry, 2020, 90(3), 470-475
合成路线:1 步
反应条件:
参考文献:
Unravel the surface active sites on Cu/MgLaO solid base catalyst by DRIFT spectroscopy and adsorption techniques for the synthesis of triazoles by click reaction
Bilakanti, Vishali; Boosa, Venu; Gutta, Naresh ; Velisoju, Vijay Kumar ; Inkollu, Sreedhar; et al, Molecular Catalysis, 2019, 476,
合成路线:1 步
反应条件:
参考文献:
Molecular hybridization approach for phenothiazine incorporated 1,2,3-triazole hybrids as promising antimicrobial agents: Design, synthesis, molecular docking and in silico ADME studies
Reddyrajula, Rajkumar; Dalimba, Udayakumar; Madan Kumar, S., European Journal of Medicinal Chemistry, 2019, 168, 263-282
合成路线:1 步
反应条件:
参考文献:
Molecular diversity of trimethoxyphenyl-1,2,3-triazole hybrids as novel colchicine site tubulin polymerization inhibitors
Fu, Dong-Jun; Li, Ping; Wu, Bo-Wen; Cui, Xin-Xin; Zhao, Cheng-Bin; et al, European Journal of Medicinal Chemistry, 2019, 165, 309-322
合成路线:1 步
反应条件:
参考文献:
Development of a Focused Library of Triazole-Linked Privileged-Structure-Based Conjugates Leading to the Discovery of Novel Phenotypic Hits against Protozoan Parasitic Infections
Uliassi, Elisa ; Piazzi, Lorna; Belluti, Federica; Mazzanti, Andrea; Kaiser, Marcel; et al, ChemMedChem, 2018, 13(7), 678-683
合成路线:1 步
反应条件:
参考文献:
Synthesis of Molecular Dyads and Triads Based Upon N-Annulated Perylene Diimide Monomers and Dimers
Cann, Jonathan R.; Cabanetos, Clement ; Welch, Gregory C., European Journal of Organic Chemistry, 2018, 2018(48), 6933-6943

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